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dc.contributor.authorAnderson, Peres_ES
dc.contributor.authorGonzález-Rey, Elenaes_ES
dc.contributor.authorO’Valle, Franciscoes_ES
dc.contributor.authorMartín, Franciscoes_ES
dc.contributor.authorOliver, Francisco Javieres_ES
dc.contributor.authorDelgado, M.es_ES
dc.date.accessioned2018-10-09T10:22:40Z-
dc.date.available2018-10-09T10:22:40Z-
dc.date.issued2017-01-30-
dc.identifier.citationStem Cells Internationales_ES
dc.identifier.issn1687-966X-
dc.identifier.urihttp://hdl.handle.net/10261/170813-
dc.description.abstractMultipotent mesenchymal stromal cells (MSCs) have emerged as a promising therapy for autoimmune diseases, including multiple sclerosis (MS). Administration of MSCs to MS patients has proven safe with signs of immunomodulation but their therapeutic efficacy remains low. The aim of the current study has been to further characterize the immunomodulatory mechanisms of adipose tissue-derived MSCs (ASCs) in vitro and in vivo using the EAE model of chronic brain inflammation in mice. We found that murine ASCs (mASCs) suppress T cell proliferation in vitro via inducible nitric oxide synthase (iNOS) and cyclooxygenase- (COX-) 1/2 activities. mASCs also prevented the lipopolysaccharide- (LPS-) induced maturation of dendritic cells (DCs) in vitro. The addition of the COX-1/2 inhibitor indomethacin, but not the iNOS inhibitor L-NAME, reversed the block in DC maturation implicating prostaglandin (PG) E2 in this process. In vivo, early administration of murine and human ASCs (hASCs) ameliorated myelin oligodendrocyte protein- (MOG35-55-) induced EAE in C57Bl/6 mice. Mechanistic studies showed that mASCs suppressed the function of autoantigen-specific T cells and also decreased the frequency of activated (CD11c+CD40high and CD11c+TNF-α+) DCs in draining lymph nodes (DLNs). In summary, these data suggest that mASCs reduce EAE severity, in part, through the impairment of DC and T cell function.es_ES
dc.description.sponsorshipThis work has been financed by the Instituto de Salud Carlos III, Spain (http://www.isciii.es) and Fondo Europeo de Desarrollo Regional (FEDER, http://ec.europa.eu/regional_policy/es/funding/erdf/) from the European Union, through the Research Grants PI15/00794, CP09/00228, and CPII15/00032 (Per Anderson); PI12/01097, PI15/02015, and ISCIII Red de Terapia Celular (RD12/0019/0006, http://www.red-tercel.com/) (Francisco Martin); and PS09-00928 (Mario Delgado). Mario Delgado was supported by a grant (PSE-010000-2009-3) from the Ministerio de Ciencia e Innovación, Spain (http://www.idi.mineco.gob.es/), and P09-CTS-4723 from the Junta de Andalucia (Proyecto de Excelencia). Francisco Martin is funded by the Fundación Progreso y Salud (Consejería de Salud, Junta de Andalucía, http://www.juntadeandalucia.es/fundacionprogresoysalud/).es_ES
dc.language.isoenges_ES
dc.publisherHindawi Publishing Corporationes_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.titleAllogeneic Adipose-Derived Mesenchymal Stromal Cells Ameliorate Experimental Autoimmune Encephalomyelitis by Regulating Self-Reactive T Cell Responses and Dendritic Cell Functiones_ES
dc.typeartículoes_ES
dc.identifier.doi10.1155/2017/2389753-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://www.hindawi.com/journals/sci/2017/2389753/es_ES
dc.identifier.e-issn1687-9678-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.contributor.orcidAnderson, Per [0000-0002-0958-7990]es_ES
dc.contributor.orcidGonzález-Rey, Elena [0000-0003-3917-9020]es_ES
dc.contributor.orcidO’Valle, Francisco [0000-0001-9207-2287]es_ES
dc.contributor.orcidOliver, Francisco Javier [0000-0002-8073-4711]es_ES
dc.contributor.orcidDelgado, M. [0000-0003-1893-5982]es_ES
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